EP2511408A1 - Tissu non tisse de fibre de carbone souple - Google Patents

Tissu non tisse de fibre de carbone souple Download PDF

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Publication number
EP2511408A1
EP2511408A1 EP10835815A EP10835815A EP2511408A1 EP 2511408 A1 EP2511408 A1 EP 2511408A1 EP 10835815 A EP10835815 A EP 10835815A EP 10835815 A EP10835815 A EP 10835815A EP 2511408 A1 EP2511408 A1 EP 2511408A1
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EP
European Patent Office
Prior art keywords
nonwoven fabric
carbon fiber
fiber nonwoven
resins
flexible carbon
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Application number
EP10835815A
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German (de)
English (en)
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EP2511408A4 (fr
Inventor
Naokazu Sasaki
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Nisshinbo Holdings Inc
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Nisshinbo Holdings Inc
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Publication of EP2511408A1 publication Critical patent/EP2511408A1/fr
Publication of EP2511408A4 publication Critical patent/EP2511408A4/fr
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • H01M8/04082—Arrangements for control of reactant parameters, e.g. pressure or concentration
    • H01M8/04201—Reactant storage and supply, e.g. means for feeding, pipes
    • H01M8/04216—Reactant storage and supply, e.g. means for feeding, pipes characterised by the choice for a specific material, e.g. carbon, hydride, absorbent
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/20—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising free carbon; comprising carbon obtained by carbonising processes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
    • B01J20/28014—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their form
    • B01J20/28033—Membrane, sheet, cloth, pad, lamellar or mat
    • B01J20/28038—Membranes or mats made from fibers or filaments
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00—Formation of filaments, threads, or the like
    • D01D5/0007—Electro-spinning
    • D01D5/0015—Electro-spinning characterised by the initial state of the material
    • D01D5/003—Electro-spinning characterised by the initial state of the material the material being a polymer solution or dispersion
    • D01D5/0038—Electro-spinning characterised by the initial state of the material the material being a polymer solution or dispersion the fibre formed by solvent evaporation, i.e. dry electro-spinning
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00—General methods for the manufacture of artificial filaments or the like
    • D01F1/02—Addition of substances to the spinning solution or to the melt
    • D01F1/10—Other agents for modifying properties
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/44—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/54—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polymers of unsaturated nitriles
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/88—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/94—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of other polycondensation products
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
    • D01F9/08—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material
    • D01F9/12—Carbon filaments; Apparatus specially adapted for the manufacture thereof
    • D01F9/14—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
    • D01F9/08—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material
    • D01F9/12—Carbon filaments; Apparatus specially adapted for the manufacture thereof
    • D01F9/14—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments
    • D01F9/20—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products
    • D01F9/21—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F9/22—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyacrylonitriles
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
    • D01F9/08—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material
    • D01F9/12—Carbon filaments; Apparatus specially adapted for the manufacture thereof
    • D01F9/14—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments
    • D01F9/20—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products
    • D01F9/24—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/70—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres
    • D04H1/72—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged
    • D04H1/728—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged by electro-spinning
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00—Fuel cells; Manufacture thereof
    • H01M8/02—Details
    • H01M8/0202—Collectors; Separators, e.g. bipolar separators; Interconnectors
    • H01M8/023—Porous and characterised by the material
    • H01M8/0234—Carbonaceous material
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30—Hydrogen technology
    • Y02E60/50—Fuel cells
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
    • Y10T442/681—Spun-bonded nonwoven fabric

Definitions

  • the present invention relates to a flexible carbon fiber nonwoven fabric.
  • Nonwoven fabrics composed of ultrafine carbon fibers have hitherto been widely used as impurity-removing filters and as fuel cell electrode components, including gas diffusion layers for fuel cells and electrode catalysts (see, for example, Patent Documents 1 to 7).
  • the carbon fibers which have an inherently low resistance to bending, have been made even finer in such nonwoven fabrics, the fabric is very brittle and lacks sufficient strength for processing. Accordingly, a drawback of nonwoven fabrics made of ultrafine carbon fibers is that they cannot be used alone to form such components.
  • heating to at least 800°C is generally required to carbonize organic compound, but most organic compound which serves as the carbon precursor has a glass transition point or melting point at or below 800°C. Therefore, when an ultrafine-fiber nonwoven fabric is heated, the organic fibers making up the fabric fuse or deform before the firing temperature is reached, making it impossible to maintain the shape of the fibers. Hence, in the case of phenolic resins, melting during firing is prevented using a crosslinking agent such as formaldehyde to chemically effect three-dimensional crosslinking beforehand.
  • a crosslinking agent such as formaldehyde
  • infusibilizing treatment is generally carried out wherein the fibers are gradually heated in air (in the presence of oxygen) so as to oxidize the fiber surfaces and thereby form on the fiber surfaces an organization coat which does not melt. As a result, the fiber shape remains unchanged up to the firing temperature.
  • Firing and carbonizing ultrafine fibers in this way without associated shape deformation due to melting requires the formation of a three-dimensionally crosslinked structure (thermosetting or hardening) or infusibilization.
  • Polymers that allow this to be done are limited to fibers capable of being infusibilized such as polyacrylonitrile and cellulose fibers, and thermosetting fibers such as amide and amide-imide fibers.
  • infusibilizing ultrafine fibers without associated shape deformation has required strict temperature control.
  • CNT carbon nanotubes
  • Non-Patent Document 1 A flexible carbon nanofiber has been reported in Non-Patent Document 1 (Non-Patent Document 1). This is obtained by dissolving, in methanol as the solvent: a phenolic resin, high-molecular-weight polyvinyl butyral, and also, as electrolytes, pyridine and sodium carbonate (Na 2 CO 3 ). The resulting solution is electrospun into a nanofiber nonwoven fabric, which is then subjected to crosslinking treatment with formaldehyde in a hydrochloric acid solution, neutralized and washed, then fired.
  • this production process is highly involved.
  • the resulting carbon nanofibers do exhibit a certain degree of flexibility, they break when bent in two, and thus leave something to be desired in terms of flexibility.
  • Patent Document 1 JP-A 2003-239164 Patent Document 2: JP-A 2005-240224 Patent Document 3: WO 2005/045115 Patent Document 4: JP-A 2007-70738 Patent Document 5: JP-A 2007-27319 Patent Document 6: WO 2007/052650 Patent Document 7: WO 2009/098812
  • Non-Patent Document 1 Polymer Journal, Vol. 41, No. 12, p. 1124 (2009 )
  • a further object is to provide a simple method of producing the same.
  • the inventor has conducted extensive investigations in order to achieve the above objects and has discovered as a result that when a nonwoven fabric which has been obtained by electrospinning a composition prepared by the mixture of at least two organic components, one of which is an electrospinnable polymeric substance and another of which is a different organic compound, with a transition metal is then carbonized, there can be obtained a flexible carbon fiber nonwoven fabric which has such a good resistance to folding that it does not break even when folded in two.
  • the invention provides:
  • the present invention by making it possible to impart to ultrafine carbon fibers the property of having a good resistance to bending, which has not been achievable by conventional methods, enables a flexible carbon fiber nonwoven fabric that is supple and endowed with a good processability to be provided.
  • the flexible carbon fiber nonwoven fabric of the invention does not require the type of conventional reinforcement treatment described above, and thus can be directly used in the form of a thin nonwoven fabric in a variety of applications. Also, because treatment using reagents such as acids, alkalis, hardening agents and crosslinking agents is not required during production of the nonwoven fabric, the production operations can be simplified.
  • Such a flexible carbon fiber nonwoven fabric can be advantageously used alone as a fuel cell electrode component such as a gas diffusion layer, as other electrode materials, as a support for a catalyst or for hydrogen storage particles, and also as chemical-resistant and heat-resistant filters, heat conductors, heat sinks, thermal insulation fillers, adsorbents and acoustic materials.
  • this nonwoven fabric can also be used as a hydrogen storage material.
  • the highly flexible carbon fiber nonwoven fabric of the invention is particularly advantageous when packed into high-pressure vessels for storing hydrogen. For example, when the inventive nonwoven fabric is wound into a roll, in spite of the high density of the rolled fabric, the gaps between the fibers readily form flow channels suitable for moving hydrogen in and out.
  • the flexible carbon fiber nonwoven fabric according to the present invention is obtained by carbonizing a nonwoven fabric obtained by electrospinning a composition which includes an electrospinnable polymeric substance, an organic compound differing from the polymeric substance, and a transition metal.
  • the electrospinnable polymer substance is not subject to any particular limitation and may be suitably selected from among hitherto known electrospinnable polymeric substances.
  • Illustrative examples include polyacrylonitrile resins, polyester resins, polyurethane resins, polyethylene resins, polypropylene resins, polyacrylic resins, polyether resins, polyvinylidene chloride resins, polyvinyl resins, polyamide resins, polyimide resins and polyamide-imide resins. These may be used singly, or two or more may be used in combination. Of these, to further increase the folding strength of the resulting carbon fiber nonwoven fabric, a polymeric substance containing a nitrogen atom on the molecule is preferred, and a polyacrylonitrile resin is especially preferred.
  • the resulting carbon fiber nonwoven fabric manifest a flexibility and toughness that keeps it from failing even when folded
  • the electrospinnable polymer plays the role of a "connector,” allowing the overall composition to be electrospun and also preventing the development of graphene sheets in the carbon fibers making up the resulting ultrafine carbon fiber nonwoven fabric.
  • carbon fibers having a good resistance to folding can be obtained.
  • the organic compound is a substance which differs from the above-described polymeric substance. Any of the various compounds which have hitherto been employed as carbon precursor materials may be used. Illustrative examples include phenolic resins, epoxy resins, melamine resins, urea resins, polycarbodiimide, pitch, cellulose, cellulose derivatives and lignin. These may be used singly or two or more may be used in combination. In cases where the polymeric substance used is one which does not contain a nitrogen atom, for the same reasons as indicated above, it is preferable for that the organic compound to be one which contains a nitrogen atom.
  • a transition metal is essential for achieving the desired flexibility and toughness in the carbon fiber nonwoven fabric of the invention. That is, by making use of a transition metal-containing composition, when heat is applied to a nonwoven fabric electrospun from the composition, melting can be prevented from occurring up until the firing temperature is reached, and the carbon fiber nonwoven fabric following carbonization can be conferred with a flexibility and toughness that keep the fabric from failing even when folded.
  • Such transition metals are not subject to any particular limitation, and are exemplified by titanium, cobalt, iron, nickel, copper, zirconia and platinum. Of these, titanium, iron and cobalt are preferred. These may be used singly, or two or more may be used in combination.
  • transition metals are preferably used in the form of a complex, salt, hydroxide, sulfate or organic oxide.
  • tetraalkoxytitaniums such as tetra-n-butoxytitanium
  • titanium halides such as titanium(III) chloride and titanium(IV) chloride
  • organic acid salts such as the ammonium salt of titanium lactate
  • cobalt halides such as cobalt(II) chloride, cobalt(III) chloride, cobalt(II) bromide, cobalt(II) fluoride, cobalt(III) fluoride, cobalt(II) iodide and cobalt(II) iodate
  • organic acid salts of cobalt such as cobalt(II) acetate and cobalt(II) octanoate
  • cobalt(II) hydroxide cobalt(II) nitrate and cobalt(III) n
  • the contents of the above polymeric substance, organic compound and transition metal in the composition used to produce the carbon fiber nonwoven fabric of the invention are not subject to any particular limitation, provided the composition is capable of being electrospun, although it is preferable for the polymeric substance to be included in an amount of from 1.0 to 15 parts by weight, especially from 1.5 to 15 parts by weight, for the organic compound to be included in an amount of from 1.0 to 15 parts by weight, especially from 1.5 to 15 parts by weight, and for the transition metal to be included in an amount (weight of metal) of from 0.1 to 2 parts by weight, especially from 0.1 to 1.5 parts by weight. Any suitable method may be used to prepare the composition, so long as each of the above ingredients is mixed in accordance with common practice. The respective ingredients may be mixed in any suitable order.
  • a solvent which is capable of dissolving the resin to be used may be suitably selected and employed as this solvent.
  • solvents which may be used include water, acetone, methanol, ethanol, propanol, isopropanol, toluene, benzene, cyclohexane, cyclohexanone, tetrahydrofuran, dimethylsulfoxide, 1,4-dioxane, carbon tetrachloride, methylene chloride, chloroform, pyridine, trichloroethane, N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, ethylene carbonate, diethyl carbonate, propylene carbonate and acetonitrile, as well as organic acids such as formic acid, lactic acid and acetic acid.
  • solvents may be used singly, or two or more may be mixed and used together. This solvent may be included in any order. That is, it may be mixed together with the various above ingredients or it may be added after the above composition has been prepared.
  • Electrospinning is a process in which, as an electrically charged electrospinning dope (electrospinning solution) is spun within an electrical field, the dope is explosion up by forces of repulsion between the electrical charges, resulting in the formation of a very fine fibrous material composed of the resin.
  • a nozzle for ejecting the dope serving as a first electrode and a collector serving as a second electrode a high voltage of from several thousands to several tens of thousands of volts is applied to the dope, causing the dope to be discharged as a jet from the nozzle. Due to the high-speed jet and subsequent folding and expansion of the jet within the electrical field, the discharged dope forms into very fine fibers which collect on the collector surface as an ultrafine fiber nonwoven fabric.
  • the resulting ultrafine fiber nonwoven fabric is then fired to give an ultrafine carbon fiber nonwoven fabric.
  • the fiber surface may be oxidized and subjected to thermosetting and infusibilizing treatment as in the prior art.
  • the heating temperature is not subject to any particular limitation, so long as infusibilization is possible.
  • the method used may be one in which the temperature is raised from room temperature to about 300°C over a period of about 2 to about 10 hours, after which the same temperature is maintained for a period of from about 30 minutes to about 3 hours.
  • the ultrafine fiber nonwoven fabric obtained as described above may be rendered into an ultrafine carbon fiber nonwoven fabric without melting and uniting of the fibers by gradual heating to the firing temperature of about 800 to about 1,500°C.
  • the temperature rise rate may be set as suitable, such as from about 1°C/min to 10°C/min. Temperature control need not be very strict.
  • the resulting ultrafine carbon fiber nonwoven fabric of the invention is a flexible carbon fiber nonwoven fabric which has a resistance to folding sufficient to not break even when folded in two. Moreover, this flexibility is retained even after the metal atoms have been removed from the resulting carbon fiber nonwoven fabric. It appears from this that the transition metal has the effect of building, in the course of carbonization, a structure having a good resistance to folding. Removal of the metal atoms may be carried out by, for example, acid treatment. Such acid treatment may be carried out by exposing the carbon fiber nonwoven fabric to a single inorganic acid such as hydrochloric acid, nitric acid or sulfuric acid, or to a mixed acid composed of a mixture of such inorganic acids. Accordingly, in cases where the carbon fiber nonwoven fabric of the invention are to be used in applications which are adversely affected by the presence of metal components, the metal components should be removed by acid treatment.
  • acid treatment may be carried out by exposing the carbon fiber nonwoven fabric to a single inorganic acid such as hydrochloric acid,
  • the carbon fibers making up the ultrafine carbon fiber nonwoven fabric of the invention have a fiber diameter of preferably from 0.1 to 15 ⁇ m, more preferably from 0.1 to 10 ⁇ m, and even more preferably from 0.1 to 1 ⁇ m.
  • the carbon fibers have a pore size, as measured by the bubble point method, of preferably 5 ⁇ m or less, and a pore size at the surface of preferably from 0.4 to 50 nm.
  • the fibers have at the surface a micropore (2 nm and smaller) surface area of preferably from 27 to 2,700 m 2 /g, and have a BET specific surface area of preferably from 30 to 3,000 m 2 /g.
  • the carbon fiber nonwoven fabric has a basis weight of preferably from 0.3 to 100 g/m 2 , a thickness of preferably from 5 to 500 ⁇ m, and a bulk density of preferably from 0.06 to 0.3 g/cm 3 .
  • the bending stiffness of the nonwoven fabric as measured by Method B (slide method) described in JIS L 1096, is preferably from 0.0005 to 50 mN ⁇ cm.
  • the gas permeability of the nonwoven fabric as measured by Method A (Frazier method) described in JIS L 1096, is preferably from 0.5 to 300 mL/sec/cm 2 .
  • the ratio Id/Ig of the peak intensity Id near 1,355 cm -1 to the peak intensity Ig near 1,580 cm -1 which indicates the degree of graphitization as measured by Raman spectroscopy, is preferably in a range of from 0.7 to 1.3. Within this range, the crystalline structure of graphite is disordered and approaches the state of noncrystalline amorphous carbon, meaning that the carbon fiber nonwoven fabric has an even better flexibility.
  • the sizes of 50 randomly selected fibers examined under an electron microscope (JSM-67010F, manufactured by JEOL, Ltd.) were measured, and the average fiber diameter was determined.
  • the thickness was measured at ten random points, and the average thickness of the fabric was determined.
  • An electrospinning dope was prepared by mixing together and dissolving 2.7 wt % of polyacrylonitrile (abbreviated below as "PAN,” available as “Barex” from Mitsubishi Chemical Corporation), 3.0 wt % of phenolic resin (abbreviated below as “Ph,” available as “PSK-2320” from Gunei Chemical Industry Co., Ltd.) and 3.5 wt % of titanium(IV) butoxide (available from Aldrich Co.) in 90.8 wt % of dimethylformamide (available from Wako Pure Chemical Industries, Ltd.; guaranteed reagent).
  • PAN polyacrylonitrile
  • Ph phenolic resin
  • Ti(IV) butoxide available from Aldrich Co.
  • the electrospinning dope obtained as described above was set in an electrospinning system (ESP-2300, manufactured by Fuence Co., Ltd.) and electrospun at a needle outlet diameter of 0.5 mm, an applied voltage of 17 kV, an extrusion pressure of 7 kPa and a relative humidity of 50% (25°C), thereby forming an ultrafine fiber nonwoven fabric built up of filaments having a diameter of about 600 nm.
  • ESP-2300 manufactured by Fuence Co., Ltd.
  • Thermosetting treatment was carried out by placing the resulting ultrafine fiber nonwoven fabric in an oven, ramping the oven from room temperature to 250°C over a period of 1.5 hours, and then additionally holding the oven at 250°C for 1 hour. After thermosetting treatment, the nonwoven fabric was examined under an electron microscope. FIG. 1 shows an electron micrograph of the fabric. As a result, it was confirmed that there was no change in the fiber shape and that the fibers had not melted together and united.
  • the ultrafine fiber nonwoven fabric was subjected to carbonizing treatment under the following conditions, giving an ultrafine carbon fiber nonwoven fabric.
  • a flask was charged with 30.93 g of acrylonitrile (available from Wako Pure Chemical Industries, Ltd.), 4.07 g of methacrylic acid (Wako Pure Chemical Industries) and 300 mL of pure water, following which deaeration (oxygen removal) was carried out by bubbling through nitrogen gas.
  • the flask contents were then heated to 70°C, following which a solution of 100 mg of potassium peroxodisulfate (Wako Pure Chemical Industries) dissolved in 50 mL of pure water was poured in under stirring. Stirring was continued for 4 hours, after which the cloudy solution was concentrated and finally dried in vacuo, giving about 20 g of a polyacrylonitrile-polymethacrylic acid copolymer (referred to below as "PAN-MAA").
  • PAN-MAA polyacrylonitrile-polymethacrylic acid copolymer
  • An electrospinning dope was prepared by mixing together and dissolving 1.5 wt % of the PAN-MAA obtained as described above, 1.5 wt % of Ph and 0.4 wt % of titanium(IV) tetrachloride (Aldrich Co.) in 96.6 wt % of dimethylformamide (Wako Pure Chemical Industries; guaranteed reagent).
  • Electrospinning was carried out under the same conditions as in Example 1, forming an ultrafine fiber nonwoven fabric built up of filaments having a diameter of about 200 nm.
  • thermosetting treatment carried out in Example 1 was omitted. Instead, the ultrafine fiber nonwoven fabric obtained after electrospinning was heat-treated under the following conditions, giving an ultrafine carbon fiber nonwoven fabric.
  • An electrospinning dope was prepared by mixing together and dissolving 15 wt % of PAN, 15 wt % of Ph and 4.0 wt % of titanium(IV) tetrachloride (Aldrich Co.) in 66 wt % of dimethylformamide (Wako Pure Chemical Industries; guaranteed reagent).
  • Electrospinning was carried out under the same conditions as in Example 1, forming an ultrafine fiber nonwoven fabric built up of filaments having a diameter of about 15 ⁇ m.
  • Example 2 Heat treatment was carried out under the same conditions as in Example 2, giving an ultrafine carbon fiber nonwoven fabric.
  • the resulting ultrafine carbon fiber nonwoven fabric was examined under an electron microscope, from which it was confirmed that the fibers had not melted together and united.
  • the fiber diameter was about 10 ⁇ m.
  • the nonwoven fabric had a thickness of 20 ⁇ m.
  • An electrospinning dope was prepared by mixing together and dissolving 1.5 wt % of PAN, 1.5 wt % of Ph and 0.4 wt % of cobalt(II) chloride (Aldrich Co.) in 96.6 wt % of dimethylformamide (Wako Pure Chemical Industries; guaranteed reagent).
  • Electrospinning was carried out under the same conditions as in Example 1, forming an ultrafine fiber nonwoven fabric built up of filaments having a diameter of about 500 nm.
  • Example 2 Heat treatment was carried out under the same conditions as in Example 2, giving an ultrafine carbon fiber nonwoven fabric.
  • the resulting ultrafine carbon fiber nonwoven fabric was examined under an electron microscope, from which it was confirmed that the fibers had not melted together and united.
  • the fiber diameter was about 400 nm.
  • the nonwoven fabric had a thickness of 20 ⁇ m.
  • An electrospinning dope was prepared by mixing together and dissolving 1.5 wt % of PAN, 1.5 wt % of Ph and 0.5 wt % of iron(III) chloride (Aldrich Co.) in 96.5 wt % of dimethylformamide (Wako Pure Chemical Industries; guaranteed reagent).
  • Electrospinning was carried out under the same conditions as in Example 1, forming an ultrafine fiber nonwoven fabric built up of filaments having a diameter of about 500 nm.
  • Example 2 Heat treatment was carried out under the same conditions as in Example 2, giving an ultrafine carbon fiber nonwoven fabric.
  • the resulting ultrafine carbon fiber nonwoven fabric was examined under an electron microscope, from which it was confirmed that the fibers had not melted together and united.
  • the fiber diameter was about 400 nm.
  • the nonwoven fabric had a thickness of 20 ⁇ m.
  • An electrospinning dope was prepared by mixing together and dissolving 1.5 wt % of PAN and 1.5 wt % of Ph in 97.0 wt % of dimethylformamide (Wako Pure Chemical Industries; guaranteed reagent).
  • Electrospinning was carried out under the same conditions as in Example 1, forming an ultrafine fiber nonwoven fabric built up of filaments having a diameter of about 500 nm.
  • Thermosetting treatment was carried out under the same conditions as in Example 1, but melting of the fibers was observed near 150°C, following which the fibers melted completely, as a result of which the nonwoven fabric shape could not be retained. Accordingly, the ultrafine fiber nonwoven fabric which was obtained as described above was immersed for 2 hours at 98°C in an aqueous solution (hardening solution) containing 15 wt % of hydrogen chloride and 8 wt % of formaldehyde, following which the fabric was neutralized, rinsed with water and dried, then subjected to hardening treatment.
  • aqueous solution hardening solution
  • Carbonizing treatment was carried out under the same conditions as in Example 1. Following treatment, the ultrafine carbon fiber nonwoven fabric was examined under an electron microscope, from which it was confirmed that the fibers had not melted together and united. The fiber diameter was about 400 nm. The nonwoven fabric had a thickness of 20 ⁇ m.
  • Non-Patent Document 1 pp. 1124-1128, Table 1, "P12"
  • An electrospinning dope was prepared by mixing together and dissolving 29.4 wt % of Ph and 0.6 wt % of polyvinyl butyral (Wako Pure Chemical Industries; average degree of polymerization, about 2,300 to 2,500; abbreviated below as "PVB") in 70.0 wt % of methanol (Wako Pure Chemical Industries; guaranteed reagent).
  • PVB polyvinyl butyral
  • electrospinning was carried out under the same conditions as in Example 1, forming an ultrafine fiber nonwoven fabric built up of filaments having a diameter of about 1,380 nm.
  • the ultrafine fiber nonwoven fabric obtained as described above was immersed at 98°C for 2 hours in an aqueous solution (hardening solution) containing 15 wt % of hydrogen chloride and 8 wt % of formaldehyde. The fabric was then taken out and rinsed with water, neutralized with 3% ammonia water at 60°C for 30 minutes, rinsed with water again, and dried, giving a Ph-PVB ultrafine fiber nonwoven fabric.
  • thermosetting treatment was carried out under the same conditions as in Example 1, melting of the fibers was observed near 150°C, following which the fibers melted completely, as a result of which the nonwoven fabric shape could not be retained.
  • Carbonizing treatment was carried out under the same conditions as in Example 1. Following treatment, the ultrafine carbon fiber nonwoven fabric was examined under an electron microscope, from which it was confirmed that the fibers had not melted together and united. The fiber diameter was about 1,230 nm. The nonwoven fabric had a thickness of 20 ⁇ m.
  • Non-Patent Document 1 pp. 1124-1128, Table 1, "P25"
  • An electrospinning dope was prepared by mixing together and dissolving 7.9 wt % of Ph, 2.0 wt % of PVB, 54.0 wt % of methanol (Wako Pure Chemical Industries; guaranteed reagent), 36.0 wt % of pyridine (Wako Pure Chemical Industries; guaranteed reagent) and 0.1 wt % of sodium carbonate (Wako Pure Chemical Industries; guaranteed reagent).
  • electrospinning was carried out under the same conditions as in Example 1, forming an ultrafine fiber nonwoven fabric built up of filaments having a diameter of about 140 nm.
  • the ultrafine fiber nonwoven fabric obtained as described above was immersed at 98°C for 2 hours in an aqueous solution (hardening solution) containing 15 wt % of hydrogen chloride and 8 wt % of formaldehyde. The fabric was then taken out and rinsed with water, neutralized with 3% ammonia water at 60°C for 30 minutes, rinsed with water again, and dried, giving a Ph-PVB ultrafine fiber nonwoven fabric.
  • thermosetting treatment was carried out under the same conditions as in Example 1, melting of the fibers was observed near 150°C, following which the fibers melted completely, as a result of which the nonwoven fabric shape could not be retained.
  • Example 1 Carbonizing treatment was carried out under the same conditions as in Example 1. Following treatment, the ultrafine carbon fiber nonwoven fabric was examined under an electron microscope, from which it was confirmed that the fibers had not melted together and united. The fiber diameter was about 110 nm. The nonwoven fabric had a thickness of 20 ⁇ m. Above Examples 1 to 5 and Comparative Examples 1 to 3 are summarized in Table 1.
  • the ultrafine carbon fiber nonwoven fabrics obtained in Examples 1 to 5 and Comparative Examples 1 to 3 were subjected to a folding test, a folding test after concentrated hydrochloric acid treatment (in Examples 1 to 5), measurement of the specific surface area and Raman analysis by the methods described below. The results are presented in Table 2.
  • Each of the ultrafine carbon fiber nonwoven fabrics (size of specimens: 10 cm x 10 cm) obtained in Examples 1 to 5 and Comparative Examples 1 to 3 was folded in two, clamped between two stainless steel plates and a load of 98 kPa (1 kgf/cm 2 ) was applied. The nonwoven fabric was then examined to determine whether breaking had occurred.
  • FIG. 4 shows an electron micrograph of the folded area of the ultrafine carbon fiber nonwoven fabric obtained in Example 1
  • FIG. 5 shows an electron micrograph of the folded area of the ultrafine carbon fiber nonwoven fabric obtained in Comparative Example 3.
  • the ultrafine carbon fiber nonwoven fabrics obtained in Examples 1 to 5 and Comparative Examples 1 to 3 were shredded.
  • the specific surface area was determined by using the BET method to measure the adsorption of 77 K nitrogen and the pore size distribution was determined by the MP method.
  • the pore size distributions in Examples 4 and 5 and Comparative Example 1 because the presence of mesopores was apparent from the adsorption isotherms, mesopores were also determined by additionally using the BJH method.
  • the ultrafine carbon fiber nonwoven fabrics obtained in Examples 1 to 5 and Comparative Examples 1 to 3 were shredded, and measurement was carried out using a micro-laser Raman spectroscope (Horiba Jobin Yvon Co., Ltd.; LabRAM HR-800) and using an argon laser (wavelength, 532 nm).
  • the ratio Id/Ig of the peak intensity of the D band near 1,355 cm -1 (Id) to the peak intensity of the G band near 1,580 cm -1 (Ig) was determined from the measurement results.
  • An electrospinning dope was prepared by mixing together and dissolving 1.5 wt % of PAN-MAA, 1.5 wt % of Ph and 2.7 wt % of titanium(IV) tetrachloride in 94.3 wt % of dimethylformamide (Wako Pure Chemical Industries; guaranteed reagent).
  • Electrospinning was carried out under the same conditions as in Example 1, forming an ultrafine fiber nonwoven fabric having a thickness of about 6 ⁇ m built up of filaments having a diameter of about 300 nm.
  • the ultrafine fiber nonwoven fabric obtained after electrospinning was heat-treated under the following conditions, giving an ultrafine carbon fiber nonwoven fabric.
  • an ultrafine carbon fiber nonwoven fabric was produced under the same conditions as in Example 6.
  • thermosetting and firing were carried out under the same conditions as in Example 6, giving an ultrafine carbon fiber nonwoven fabric having a fiber diameter of about 200 nm and a thickness of about 100 ⁇ m.
  • an ultrafine carbon fiber nonwoven fabric was produced under the same conditions as in Example 6.
  • thermosetting and firing were carried out under the same conditions as in Example 6, giving an ultrafine carbon fiber nonwoven fabric having a fiber diameter of about 200 nm and a thickness of about 500 ⁇ m.
  • an ultrafine carbon fiber nonwoven fabric was produced under the same conditions as in Example 6.
  • thermosetting and firing were carried out under the same conditions as in Example 6, thereby giving an ultrafine carbon fiber nonwoven fabric having a fiber diameter of about 200 nm and a thickness of about 450 ⁇ m.
  • the nonwoven fabric was then pressed, and thereby compressing it to a thickness of 300 ⁇ m.
  • An electrospinning dope was prepared by mixing together and dissolving 3 wt % of PAN and 97.0 wt % of dimethylformamide (Wako Pure Chemical Industries; guaranteed reagent).
  • Electrospinning was carried out under the same conditions as in Example 1, forming an ultrafine fiber nonwoven fabric having a thickness of about 120 ⁇ m built up of filaments having a diameter of about 300 nm.
  • Thermosetting treatment was carried out under the same conditions as in Example 1.
  • the treated nonwoven fabric was examined under an electron microscope, from which it was confirmed that there was no change in the shape of the fibers and that the fibers had not melted together and united.
  • Example 2 Aside from setting the holding temperature to 1,500°C, carbonizing treatment was carried out under the same conditions as in Example 1. Following treatment, the ultrafine carbon fiber nonwoven fabric was examined under an electron microscope, from which it was confirmed that the fibers had not melted together and united. The fiber diameter was about 200 nm. The nonwoven fabric had a thickness of about 100 ⁇ m. After firing, the nonwoven fabric was very brittle, making it impossible to measure the maximum pore size by the subsequently described bubble point method or to measure the bending stiffness and gas permeability.
  • An electrospinning dope was prepared by mixing together and dissolving 3 wt % of the PAN-MAA prepared in Example 2 and 2.7 wt % of cobalt(II) chloride (Aldrich Co.) in 94.3 wt % of dimethylformamide (Wako Pure Chemical Industries; guaranteed reagent).
  • Electrospinning was carried out under the same conditions as in Example 1, forming an ultrafine fiber nonwoven fabric having a thickness of about 120 ⁇ m built up of filaments having a diameter of about 300 nm.
  • Thermosetting treatment was carried out under the same conditions as in Example 1.
  • the treated nonwoven fabric was examined under an electron microscope, from which it was confirmed that there was no change in the shape of the fibers and that the fibers had not melted together and united.
  • Example 2 Aside from setting the holding temperature to 1,500°C, carbonizing treatment was carried out under the same conditions as in Example 1. Following treatment, the ultrafine carbon fiber nonwoven fabric was examined under an electron microscope, from which it was confirmed that the fibers had not melted together and united. The fiber diameter was about 200 nm. The nonwoven fabric had a thickness of about 100 ⁇ m. After firing, the nonwoven fabric was very brittle, making it impossible to measure the maximum pore size by the bubble point method or to measure the bending stiffness and gas permeability. The fibers were examined under a transmission electron microscope (TEM) to determine the cause of the above, whereupon the development of graphene sheets was observed. FIG. 6 shows a TEM image. The development of graphene sheets and the layer structure these form presumably triggered structural changes at the interior of the fibers, making the fibers brittle to folding. Above Examples 6 to 9 and Comparative Examples 4 and 5 are summarized in Table 3.
  • the ultrafine carbon fiber nonwoven fabrics obtained in Examples 6 to 9 and Comparative Examples 4 and 5 were subjected to a folding test and measurement of the basis weight, bubble point maximum pore size, gas permeability, bulk density, bending stiffness and electrical resistivity by the methods described below. The results are presented in Table 4.
  • a nonwoven fabric specimen having a size of 20 cm x 20 cm was dried, following which the weight was measured.
  • the maximum pore size was determined by the bubble point method using a porous material automated pore size distribution measuring system (Automated Perm Porometer, from Porous Materials, Inc.).
  • the nonwoven fabric was clamped between gold-plated electrode plates, each having a radius of 3 cm and a thickness of 1 cm, the electrical resistivity under the application of a load of 10 kPa was measured, and the electrical resistivity in the thickness direction per unit area was calculated.
  • the ultrafine carbon fiber nonwoven fabric produced in Example 1 was shredded, and the hydrogen adsorption isotherm curve at 77 K was measured for 150 mg of the shredded fabric using a specific surface area measuring instrument (Belsorp Max, from Bel Japan, Inc.).
  • the amount of hydrogen adsorbed per gram was determined from the hydrogen adsorption volume obtained by measurement (cm 3 /g ⁇ STP, where STP is 101.325 kPa and 0°C (273 K)), and the relationship between the amount of adsorbed hydrogen and the measurement pressure (mmHg) was plotted on a graph. The results are shown in FIG. 7 .
  • ultrafine carbon fiber nonwoven fabric can be regarded as advantageous when considering the storage of hydrogen at high pressure.

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CN102652192A (zh) 2012-08-29
US8993199B2 (en) 2015-03-31
WO2011070893A1 (fr) 2011-06-16
JP5672239B2 (ja) 2015-02-18
CN102652192B (zh) 2014-12-24
CA2782274A1 (fr) 2011-06-16
US20120251925A1 (en) 2012-10-04
JPWO2011070893A1 (ja) 2013-04-22

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